| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:82429418-82429663 | Common:1; Rare:136; Clinvar:10; Clinvar (benign):6 | ||||
| chr4:82429831-82430065 | Common:1; Rare:61 | ||||
| chr4:82430372-82430598 | Common:1; Rare:83 | ||||
| chr4:82562071-82562471 | Common:3; Rare:103 | ||||
| chr4:82798764-82799062 | Common:5; Rare:102 | ||||
| chr4:82891109-82891456 | Common:2; Rare:126 | ||||
| chr4:82900473-82900843 | Rare:117 | ||||
| chr4:82901144-82901280 | Common:1; Rare:30 | ||||
| chr4:83010195-83010337 | Rare:26 | ||||
| chr4:83010735-83010921 | Rare:28 | ||||
| chr4:83010957-83011121 | Rare:21 | ||||
| chr4:83012871-83013296 | Common:2; Rare:111 | ||||
| chr4:83034836-83035261 | Common:1; Rare:110 | ||||
| chr4:83284408-83284602 | Common:2; Rare:73; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:83284724-83284913 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 |